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Caproic acid

$43

  • Brand : BIOFRON

  • Catalogue Number : AV-PC0061

  • Specification : 98%

  • CAS number : 142-62-1

  • Formula : C6H12O2

  • Molecular Weight : 116.16

  • Volume : 20mg

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Catalogue Number

AV-PC0061

Analysis Method

HPLC,NMR,MS

Specification

98%

Storage

2-8°C

Molecular Weight

116.16

Appearance

Botanical Source

Structure Type

Category

SMILES

CCCCCC(=O)O

Synonyms

IUPAC Name

Applications

Density

1.0±0.1 g/cm3

Solubility

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

Flash Point

104.4±0.0 °C

Boiling Point

204.6±3.0 °C at 760 mmHg

Melting Point

?4 °C(lit.)

InChl

InChI=1S/C6H12O2/c1-2-3-4-5-6(7)8/h2-5H2,1H3,(H,7,8)

InChl Key

FUZZWVXGSFPDMH-UHFFFAOYSA-N

WGK Germany

RID/ADR

HS Code Reference

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:142-62-1) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

32199968

Title

RIFM fragrance ingredient safety assessment, hexanoic acid, CAS Registry Number 142-62-1

Author

A M Api 1, D Belsito 2, S Biserta 1, D Botelho 1, M Bruze 3, G A Burton Jr 4, J Buschmann 5, M A Cancellieri 1, M L Dagli 6, M Date 1, W Dekant 7, C Deodhar 1, A D Fryer 8, S Gadhia 1, L Jones 1, K Joshi 1, A Lapczynski 1, M Lavelle 1, D C Liebler 9, M Na 1, D O'Brien 1, A Patel 1, T M Penning 10, G Ritacco 1, F Rodriguez-Ropero 1, J Romine 1, N Sadekar 1, D Salvito 1, T W Schultz 11, F Siddiqi 1, I G Sipes 12, G Sullivan 13, Y Thakkar 1, Y Tokura 14, S Tsang 1

Publish date

2020 Apr 15

PMID

31898751

Abstract

Polycyclic aromatic hydrocarbons (PAHs) and naphthenic acids (NAs) are toxic contaminants of environmental concern found in process water and mature fine tailings, or tailings, from the oil sands industry. BioTiger™, a patented microbial consortium of twelve natural environmental isolates, was found to cometabolically biodegrade the NA hexanoic acid and the PAH phenanthrene in the presence of tailings. Hexanoamide was found to be produced and consumed during cometabolism of hexanoic acid. Mechanistic analysis demonstrated three of the BioTiger™ strains generated biosurfactants with the bacterial adhesion to hydrocarbons assay, seven with the methylene blue active substances assay, and nine with a hemolysis assay. Serial transfers of the BioTiger™ consortium demonstrated the stability of hexanoic acid degradation over several generations. The results demonstrate that BioTiger™ cometabolically biodegrades combinations of phenanthrene and hexanoic acid in tailings. This work reveals the potential for in situ bioremediation of tailings with this natural microbial consortium.

KEYWORDS

BioTiger™; Biosurfactants; Hexanoamide; Hexanoic acid; Mature fine tailings; Phenanthrene.

Title

Bioremediation of Hexanoic Acid and Phenanthrene in Oil Sands Tailings by the Microbial Consortium BioTiger꽓

Author

Daniel O Reddy 1, Charles E Milliken 2, Koji Foreman 3, Jasmine Fox 4, Waltena Simpson 4, Robin L Brigmon 5

Publish date

2020 Feb;

PMID

31787190

Abstract

Production of biochemicals from waste streams has been attracting increasing worldwide interest to achieve climate protection goals. Chain elongation (CE) for production of medium-chain carboxylic acids (MCCAs, especially caproate, enanthate and caprylate) from diverse biowaste has emerged as a potential economic and environmental technology for a sustainable society. The present mini review summarizes the research utilizing various synthetic or real waste-derived substrates available for MCCA production. Additionally, the microbial characteristics of the CE process are surveyed and discussed. Considering that a large proportion of recalcitrantly biodegradable biowaste and residues cannot be further utilized by CE systems and remain to be treated and disposed, we propose here a loop concept of bioconversion of biowaste to MCCAs making full use of the biowaste with zero emission. This could make possible an alternative technology for synthesis of value-added products from a wide range of biowaste, or even non-biodegradable waste (such as, plastics and rubbers). Meanwhile, the remaining scientific questions, unsolved problems, application potential and possible developments for this technology are discussed.

KEYWORDS

Chain elongation; Electron donors; Functional microbes; Medium-chain carboxylic acids; Organic waste; Waste valorization.

Title

Road to full bioconversion of biowaste to biochemicals centering on chain elongation: A mini review

Author

Wenhao Han 1, Pinjing He 2, Liming Shao 2, Fan Lu 3

Publish date

2019 Dec;